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Journal of Ethnopharmacology, ISSN 0378-8741, 03/2018, Volume 213, pp. 230 - 255
The medicinal plant How. (MO) and its root have long been used in traditional medicines in China and northeast Asia as tonics for nourishing the kidney,... 
Inulotriose (PubChemCID: 101708615) | 2-hydroxy-3-hydroxymethylanthraquinone (PubChemCID:44445519) | Benzeneacetaldehyde (PubChem CID:998) | 2-hydroxy-3-hydroxymethy-lanthraquinone (PubChem CID:44445519) | Ar-Curcumene (PubChem CID:92139) | 1-hydroxy-anthraquinone (PubChemCID:8512) | Traditional uses | 1-hexanol (PubChem CID:8103) | Rubiadin (PubChemCID: 124062) | Alizarin-2-Methyl ether (PubChemCID:23669622) | 1-kestose (PubChemCID: 440080) | Succinic acid (PubChemCID:1110) | 2-hydroxy-1-methoxy-anthraquinone (PubChemCID:80309) | L-borneol (PubChem CID:10049) | 3-methyl-benzaldehyde (PubChem CID:12105) | L-Camphor (PubChem CID:230921) | 1-hydroxy-2-methyl anthraquinone (PubChemCID:160817) | Hexasaccharide (PubChemCID: 3082034) Heptasaccharide (PubChem CID: 44630346) | Morindolide (PubChemCID:10397184) | α-zingiberene (PubChem CID:92776) | Digiferruginol (PubChemCID:32209) | N-Nonanal (PubChem CID:31289) | Phytochemistry | Lucidin-ѡ-Ethyl ether (PubChem CID:28578) | Morinda officinalis How | β-sitosterol (PubChemCID: 222284) | (Z,Z)-9,12-octadecadienoic acid (PubChem CID:5280450) | Sucrose (PubChemCID: 5988) | Rubiadin-1-Methyl ether (PubChemCID:96191) | Asperuloside tetraacetate (PubChemCID:443336) | Daucosterol (PubChem CID:5742590) | Tectoquinone (PubChemCID:6773) | Scopoletin (PubChem CID:5280460) | Trisaecharide (PubChemCID: 10206531) | Pentadecanoic acid (PubChem CID:13849) | β-bisabolene (PubChem CID:10104370) | Morofficinaloside (PubChemCID:10453987) | Physcion (PubChemCID: 10639) | Fumaric acid (PubChemCID:444972) | 1, 3-dihydroxy-2-methoxyanthraquinone (PubChemCID:14189688) | Asperulosidic acid (PubChemCID: 11968867) | N-hexadecanoic acid (PubChem CID:985) | Deacetyl asperulosidic acid (PubChemCID: 12315349) | β-sesquiphelandrene (PubChem CID:12315492) | Mannose (PubChemCID:18950) | Pharmacology | 2-methoxyanthraquinone (PubChemCID:18646) | Nystose (PubChemCID:166775) | Bicyclo[4,2,0]octa-1,3,5-trien-7-O (PubChem CID:354193) | Inulopentaose (PubChemCID:101110146) | Asperuloside (PubChemCID:84298) | Stigmasterol (PubChem CID: 5280394) | Monotropein (PubChemCID:73466) | Inulotetraose (PubChem CID: 101708615) | APOPTOSIS | CHEMISTRY, MEDICINAL | OLIGOSACCHARIDES | MEDICINE | PLANT SCIENCES | BONE LOSS | CHEMICAL-CONSTITUENTS | ANTHRAQUINONES | INTEGRATIVE & COMPLEMENTARY MEDICINE | ROOTS | PHARMACOLOGY & PHARMACY | STRESS | POLYSACCHARIDE | EXTRACT | Index Medicus
Journal Article
Journal Article
Journal Article
EXPERIMENTAL CELL RESEARCH, ISSN 0014-4827, 05/2007, Volume 313, Issue 9, pp. 1911 - 1920
The transient receptor potential channel of melastatin type 8 (TRPM8), which is gated by low (< 25 degrees C) temperature and chemical compounds, is regulated... 
PROTEIN-KINASE-C | VANILLOID VR1 RECEPTORS | ACTIVATION | calcium | ROOT GANGLION NEURONS | cannabinoid | TRPV1 | CELL BIOLOGY | CAPSAICIN RECEPTOR | ONCOLOGY | PROSTATE-CANCER | MENTHOL | TRPM8 | ION CHANNELS | COLD | TRPV1 CHANNELS | Cannabinoid Receptor Modulators - metabolism | Cannabinoid Receptor Modulators - pharmacology | Humans | Dose-Response Relationship, Drug | Arachidonic Acids - metabolism | Ion Channel Gating - physiology | Transfection | Pyrimidinones - pharmacology | Cell Membrane - metabolism | TRPM Cation Channels - drug effects | Cyclic AMP - metabolism | Cell Membrane - drug effects | Cyclic AMP-Dependent Protein Kinases - drug effects | Dopamine - metabolism | Endocannabinoids | Cyclic AMP-Dependent Protein Kinases - metabolism | Cell Line | Benzaldehydes - chemistry | Colforsin - pharmacology | 8-Bromo Cyclic Adenosine Monophosphate - pharmacology | Dopamine - pharmacology | Enzyme Inhibitors - pharmacology | Polyunsaturated Alkamides - metabolism | Arachidonic Acids - pharmacology | Receptor, Cannabinoid, CB1 - metabolism | Dopamine - analogs & derivatives | Menthol - pharmacology | Receptor, Cannabinoid, CB1 - genetics | Signal Transduction - drug effects | Drug Interactions - physiology | Polyunsaturated Alkamides - pharmacology | Receptor, Cannabinoid, CB1 - drug effects | TRPM Cation Channels - genetics | Signal Transduction - physiology | TRPM Cation Channels - metabolism | Ion Channel Gating - drug effects
Journal Article
Journal Article
ChemMedChem, ISSN 1860-7179, 11/2018, Volume 13, Issue 21, pp. 2297 - 2304
Journal Article
Enzyme and Microbial Technology, ISSN 0141-0229, 01/2013, Volume 52, Issue 1, pp. 68 - 76
► A Structure Activity Relationship study for laccase mediator systems was performed. ► Five quantum-chemical calculated molecular descriptors were used. ►... 
Quantum-chemistry | SAR | Prediction model | Pesticide transformation | Electron paramagnetic resonance | Laccase mediators | Radical intermediates | REDOX POTENTIALS | TRAMETES-VERSICOLOR | IMMOBILIZED LACCASE | POLYCYCLIC AROMATIC-HYDROCARBONS | NATURAL MEDIATORS | PHENOLIC-COMPOUNDS | FREE-RADICALS | FUNGAL LACCASES | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | CONTINUUM MODEL | PLEUROTUS-OSTREATUS | Fungal Proteins - chemistry | Dichlorophen - chemistry | Coumaric Acids - chemistry | Models, Chemical | Polyporales - enzymology | Dichlorophen - pharmacology | Catechols - chemistry | Vanillic Acid - pharmacology | Nitrophenols - chemistry | Nitrophenols - pharmacology | Biocatalysis - drug effects | Acetophenones - pharmacology | Catechols - pharmacology | Molecular Structure | Vanillic Acid - chemistry | Quantitative Structure-Activity Relationship | Phenols - pharmacology | Benzaldehydes - chemistry | Oxidation-Reduction | Models, Molecular | Benzaldehydes - pharmacology | Laccase - chemistry | Hydrazones - chemistry | Hydrazones - pharmacology | Laccase - metabolism | Acetophenones - chemistry | Phenols - chemistry | Protein Conformation | Decision Trees | Coumaric Acids - pharmacology | Fungal Proteins - metabolism | Oxidases | Analysis | Models | Protein kinase A | Enzymes | Transformation | Free radicals | Enthalpy | Pesticides | phenolic compounds | Radicals | Molecular modelling | Energy | Ionization | Classification | Kinetics | Redox potential | Laccase
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2015, Volume 10, Issue 5, p. e0127060
Journal Article
Journal Article
Plant Foods for Human Nutrition, ISSN 0921-9668, 9/2015, Volume 70, Issue 3, pp. 331 - 337
A comparative analysis of ethanol extracts from peel, pulp and seed of Prunus persica var. platycarpa (Tabacchiera peach) was done. The total phenol, flavonoid... 
Chemistry | Prunus persica L. Stokes ex Batsch var. platycarpa | Dietary antioxidants | Food Science | Nutrition | HPLC-ESI-MS/MS | Chemistry/Food Science, general | Phenols | Ecology | Plant Physiology | CAPACITY | FRUITS | ASSAY | PHENOLIC-COMPOUNDS | FOOD SCIENCE & TECHNOLOGY | CAROTENOIDS | PLANT SCIENCES | CULTIVARS | POLYPHENOLS | NUTRITION & DIETETICS | SOLVENTS | NECTARINE | CHEMISTRY, APPLIED | L. BATSCH PROGENY | Plant Extracts - chemistry | Gallic Acid - pharmacology | Species Specificity | Chlorogenic Acid - pharmacology | Plant Extracts - pharmacology | Humans | Chromatography, High Pressure Liquid | Biphenyl Compounds - metabolism | Tandem Mass Spectrometry | Hydroxybenzoates - pharmacology | Prunus persica - chemistry | Gallic Acid - analysis | Catechols - pharmacology | Seeds - chemistry | Antioxidants - analysis | Benzothiazoles - metabolism | Chlorogenic Acid - analysis | Hydroxybenzoates - analysis | Oxidation-Reduction | Coumaric Acids - analysis | Fruit - chemistry | Picrates - metabolism | Benzaldehydes - pharmacology | Antioxidants - pharmacology | Sulfonic Acids - metabolism | beta Carotene - metabolism | Propionates | Benzaldehydes - analysis | Catechols - analysis | Coumaric Acids - pharmacology | Antioxidants | Physiological aspects | Nutritional aspects | Research | Peach | Fenols | Arbres fruiters | Fruit trees
Journal Article
Nature Communications, ISSN 2041-1723, 08/2014, Volume 5, Issue 1, pp. 4202 - 4202
Endoplasmic reticulum (ER) stress activates the unfolded protein response and its dysfunction is linked to multiple diseases. The stress transducer IRE1 alpha... 
ACTIVATION | UNFOLDED PROTEIN RESPONSE | MESSENGER-RNA | ER STRESS | MULTIDISCIPLINARY SCIENCES | KINASE | IRE1-ALPHA | ENDOPLASMIC-RETICULUM STRESS | TRANSCRIPTION FACTOR | TRANSMEMBRANE PROTEIN | REVEALS | Small Molecule Libraries - pharmacology | Plasmacytoma - drug therapy | Humans | Coumarins - chemistry | Crystallography, X-Ray | Cell Line, Tumor - drug effects | Plasmacytoma - pathology | Structure-Activity Relationship | Ribonucleases - metabolism | DNA Mutational Analysis | Aldehydes - pharmacology | Enzyme Inhibitors - chemistry | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Membrane Proteins - metabolism | Molecular Structure | Binding Sites | Protein-Serine-Threonine Kinases - metabolism | Catalytic Domain | Benzaldehydes - chemistry | Enzyme Inhibitors - metabolism | Membrane Proteins - genetics | Enzyme Inhibitors - pharmacology | Protein-Serine-Threonine Kinases - genetics | Morpholines - pharmacology | Benzaldehydes - pharmacology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Regulatory Factor X Transcription Factors | Morpholines - chemistry | Coumarins - pharmacology | Small Molecule Libraries - chemistry | Membrane Proteins - antagonists & inhibitors | Membrane Proteins - chemistry | Protein Conformation | Protein-Serine-Threonine Kinases - chemistry | CD59 Antigens - metabolism | Aldehydes - chemistry | Index Medicus
Journal Article